CAJ | 학술논문

以6－氯－5，12－萘并萘醌为起始原料，合成了6－（4－甲氧基苯氧基）－5，12－萘并萘醌，通过元素分析、 IR、1 H NMR和EIMS对其结构进行了表征。研究表明：6－（4－甲氧基苯氧基）－5，12－萘并萘醌可以发生类似于苯氧基萘并萘醌的光异构化反应， trans－form的最大吸收峰出现在395 nm处，而ana－form在450 nm和481 nm处显示出特征双峰，并且只在408 nm处有一个等吸光点。
이6－록－5，12－내병내곤위기시원료，합성료6－（4－갑양기분양기）－5，12－내병내곤，통과원소분석、 IR、1 H NMR화EIMS대기결구진행료표정。연구표명：6－（4－갑양기분양기）－5，12－내병내곤가이발생유사우분양기내병내곤적광이구화반응， trans－form적최대흡수봉출현재395 nm처，이ana－form재450 nm화481 nm처현시출특정쌍봉，병차지재408 nm처유일개등흡광점。
6-(4-Methoxyphenoxy)-5,12-naphthacenequinone was synthesized using 6-chloro-5,12-naphthacenequinone as the starting material and its structure was confirmed using elemental analysis and the IR, 1 H NMR and MS spectra.The compound exhibited the similar photoisomerization performance with that of phenoxynaphthacenequinone.The transform had an absorption maximum at 395 nm, while the ana-form had two large absorption maxima at 450 nm and 481 nm.Only one isosbestic point was observed at 408 nm.